Variant report

Variant	rs17242358
Chromosome Location	chr8:129964873-129964874
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17241908	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55658222	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55847434	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55865336	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56330003	0.81[AMR][1000 genomes]
rs7017665	0.96[EUR][1000 genomes]
rs72728734	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72728736	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72728755	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129960000-129965200	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:129961200-129967600	Weak transcription	Dnd41	blood
3	chr8:129962400-129966200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links